IHU-Méditerranée Infection, Marseille, France.
Aix Marseille Univ., IRD, AP-HM, MEPHI, Marseille, France.
PLoS Negl Trop Dis. 2020 Dec 18;14(12):e0008947. doi: 10.1371/journal.pntd.0008947. eCollection 2020 Dec.
Leishmaniasis is among the world's most neglected diseases. Dogs are the main reservoirs/hosts of Leishmania infantum, causative agent of both canine and human visceral leishmaniosis. Canine leishmaniasis (CanL) represents a public health problem as one of the most prevalent zoonotic diseases worldwide. Current therapeutics present drawbacks; thus, there is a need for more effective, safer, and cheaper drugs. The aim of this study was to evaluate and to compare the efficacy of oral administration of artesunate or meglumine antimoniate/allopurinol in dogs with clinical leishmaniasis. Forty-two dogs with naturally occurring clinical leishmaniasis were included in this open-label, simple randomized positive-control clinical field trial with 6 months of follow-up. Dogs received meglumine antimoniate 100 mg/kg/day and allopurinol 30 mg/kg/day for 28 days (control group, n = 26) or artesunate 25 mg/kg/day for 6 days (test group, n = 16). The animals were evaluated for their clinical evolution, parasite load (by qPCR) and humoral response at different time points: 0, 30, 90, and 180 days after treatment. Data analyses showed a significant improvement in both groups in clinical scores, parasitemia and antibody titers after treatment. Compared to the control group, the artesunate group showed significantly lower clinical score (P = 0.0001), lower parasitemia (P = 0.0001) and antibody titers after 6 months of follow-up. Compared to baseline values, a rapid, significant reduction (P < 0.012) in antibody levels, 2.28- versus 3.04-fold for the control versus artesunate groups, respectively, was observed 30 days after treatment. Antibody levels continued to decrease further in the artesunate group, where 58% of cases became seronegative at the 6-month follow-up. All qPCR-positive dogs were negative after treatment with artesunate, while 14.3% remained positive with the appearance of two new cases in the control group. Artesunate was well tolerated, and no side effects were recorded. Treatment failures were similar in both groups with 27.27% (6/22), including 18.18% (4/22) mortality in the control group, versus 26.66% (4/15), including 13.33% (2/15) mortality in the artesunate group. This is the first report showing the potential of artesunate in the treatment of dogs with clinical leishmaniasis. Artesunate showed higher efficacy than the current first-line treatment for CanL without any adverse effects. It could be a good alternative chemotherapy for CanL, and may be considered for further studies in human leishmaniases. Further clinical trials are needed to confirm these findings, to determine if there are relapses after treatment and if dogs remain infective to sandflies, to define the ideal therapeutic dosage and duration of treatment with artesunate.
利什曼病是世界上最被忽视的疾病之一。狗是利什曼原虫的主要宿主/储存宿主,利什曼原虫是犬内脏利什曼病和人类内脏利什曼病的病原体。犬内脏利什曼病(CanL)是全球最普遍的人畜共患病之一,代表着一个公共卫生问题。目前的治疗方法存在缺陷;因此,需要更有效、更安全、更便宜的药物。本研究旨在评估和比较口服青蒿琥酯或葡甲胺锑/别嘌呤醇治疗临床利什曼病犬的疗效。在这项为期 6 个月的开放性、简单随机阳性对照临床现场试验中,纳入了 42 只患有自然发生的临床利什曼病的犬,共有 6 个月的随访。犬接受葡甲胺锑 100mg/kg/天和别嘌呤醇 30mg/kg/天 28 天(对照组,n=26)或青蒿琥酯 25mg/kg/天 6 天(实验组,n=16)。在不同时间点(治疗后 0、30、90 和 180 天)对动物的临床演变、寄生虫载量(通过 qPCR)和体液反应进行评估。数据分析显示,两组的临床评分、寄生虫血症和抗体滴度在治疗后均有显著改善。与对照组相比,青蒿琥酯组的临床评分显著降低(P=0.0001),寄生虫血症(P=0.0001)和抗体滴度在 6 个月的随访中也显著降低。与基线值相比,治疗后 30 天,对照组和青蒿琥酯组的抗体水平分别快速、显著降低(P<0.012),分别下降了 2.28-和 3.04 倍。在青蒿琥酯组,抗体水平进一步下降,其中 58%的病例在 6 个月的随访中变为血清阴性。所有 qPCR 阳性犬在接受青蒿琥酯治疗后均转为阴性,而对照组有 14.3%仍为阳性,并出现了 2 例新病例。青蒿琥酯耐受性良好,未记录到任何副作用。两组的治疗失败率相似,分别为 27.27%(6/22),对照组死亡率为 18.18%(4/22),而青蒿琥酯组为 26.66%(4/15),死亡率为 13.33%(2/15)。这是首次报道青蒿琥酯在治疗临床利什曼病犬方面的潜力。青蒿琥酯的疗效高于目前 CanL 的一线治疗方法,且无任何不良反应。它可能是 CanL 的一种良好的化学治疗替代药物,值得进一步研究人类利什曼病。需要进一步的临床试验来证实这些发现,以确定治疗后是否有复发,以及犬是否仍然对沙蝇具有感染力,以确定青蒿琥酯的理想治疗剂量和治疗持续时间。